Diarylacetylenes, enamines and acetylenic polymers and their production

ABSTRACT

Diarylacetylenes and diarylenamines are synthesized from a Schiff&#39;s base and an N-arylmethylheterocycle; these compounds are useful as intermediates for a variety of polymers; in particular an efficient process is provided for producing diaryl acetylenes useful in the efficient production of acetylene group-containing polymers which can be cross-linked to produce high strength polymers free of structural defects such as conventionally arise as a result of liberation of volatiles during the cross-linking.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of U.S. Patent Application Ser. No. 07/787,055 filed Nov. 4, 1991, U.S. Pat. No. 5,233,046.

BACKGROUND OF THE INVENTION

i) Field of the Invention

This invention relates to processes for producing diarylacetylenes and enamines which are valuable in the synthesis of homopolymers and copolymers, for example, poly(arylether)s, polyesters, polycarbonates and polyformals.

ii) Brief Description of Prior Art

Advanced composite materials are made from combinations of high performance fibers, such as glass, graphite, carbon, silicon carbide or ceramic fibers, arranged in close packed alignment in the polymer as a matrix. Such composite materials provide a combination of strength and modulus superior to that of structural metals and alloys on an equal weight basis. Such composites are, for example, employed in military and commercial aircraft, and space vehicles, as well as in sports equipment, in tennis racquets, shafts for golf clubs and sailboats.

These composite materials are expensive, and so their use is confined to relatively high cost items. On the other hand, even though the raw materials for these advanced composites are expensive, over 70% of the costs associated with such composites result from the processing costs for their manufacture.

In particular, the currently used manufacturing processes produce volatiles during curing of the polymer matrix and such volatiles produce voids in the matrix which act as sites for structural failure. In order to minimize void formation during evolution of volatiles, the cure must be carried out over a long period, under reduced pressure and this manufacturing requirement is a major factor in the production cost.

Acetylenic groups have been proposed in polymers in order to provide reactive sites for cross-linking the polymers when heated. The potential advantage of such acetylenic groups is that no volatiles will be produced during curing or cross-linking.

The acetylenic groups have been introduced into polymer chains as terminal groups, pendant groups or internal groups.

Acetylene precursor polymers have been reviewed by Hergenrother (P. M. Hergenrother, J. Marcromol. Sci.-Rev. Macromol. Chem. C19(1), 1-34 (1980).

Most of the polymers with terminal acetylenic groups, that have been synthesized contain unsubstituted ethynyl groups on the ends of the polymer chains and they are generally end-capped low molecular weight oligomers which are synthesized in order to provide easier processability. Reinhardt et al (B. A. Reinhardt, F. E. Arnold and M. R. Unroe, U.S. Pat. No. 4,513,131 (1985)) have synthesized the simple bis(phenylethynylphenyl)ethers as potentially thermally curable resins and studied their thermal curing properties.

Polymers containing pendant phenylethynyl groups have been synthesized and these polymers have been thermally cured. Examples are described in the afore-mentioned Hergenrother article and in U.S. Pat. No. 4,375,536 (1983) of Hergenrother.

Polymers containing internal acetylene groups have been less studied. T. Takeichi, H. Date and Y. Takayama, J. Pol. Sci. Chem. Ed. 28, 1989 (1990) describes the synthesis of polyimides containing internal acetylene groups. The authors indicating internal acetylene groups. The authors indicate that the diphenylacetylene groups must be linked in the metal position to provide effective cross-linking.

Synthesis of Diarylacetylenes

Synthetic methods are reviewed in "Comprehensive Organic Chemistry" Pergamonn Press, 1979, Vol. 1 and in The Chemistry of the Carbon-Carbon Triple Bond, Ed. Saul Patai, John Wiley & Sons 1978, Part 2.

I. Dehydrohalogenation Reactions

The most common method of synthesis is by dehydrohalogenation reactions of iodo, bromo or chloro compounds with strong bases, usually KOH, NaOH, alkoxides such as sodium methoxide or potassium tertiary butoxide or sodamide, or with hydrides, e.g. sodium hydride or with organometallic compounds such as butyl lithium. ##STR1##

The elimination of other groups, thiols, sulfides, sulfonic acids, phosphate esters, trialkyl tin hydrides and the elimination of tertiary amines in a Hofmann elimination has also been observed (pp. 776-81 of the afore-mentioned S. Patai).

II. Displacement Reactions

Copper acetylides can react with aryl halides to give diarylacetylenes (p 796 of S. Patai) and aryl halides also react with acetylenes in the presence of palladium catalysts (p 798 of S. Patai): ##STR2##

Benzotriazole, benzimidazole and triazoles have been shown by Katritzky to behave as pseudohalogens in certain reactions, (e.g. A. R. Katritzky, Q.-H. Long and P. Lue, Tetrahedron Letters, 32,3597 (1991) they have demonstrated that dienamines can be synthesized from substituted benzotriazoles by reaction with sodium hydride. ##STR3##

In this reaction the benzotriazole moiety behaves as a pseudohalogen and is eliminated with base in the same way a halogen like bromine would be. This is discussed further in a review article (A. R. Katritzky, S. Rachwal and G. J. Hutchings, Tetrahedron 47,2683 (1991).

The production of enamines is described in U.S. Pat. No. 5,011,998 (1991) of A. S. Hay et al. As described by Hay et al, the enamines are readily hydrolyzed to deoxybenzoins which in turn are readily oxidized to benzils which are useful in the production of a variety of polymers.

SUMMARY OF THE INVENTION

It is an object of this invention to provide a novel synthesis for chemical intermediates for polymer production.

It is a more particular object of this invention to provide processes for the production of diarylacetylenes,

It is a further particular object of this invention to provide a process for the production of enamines.

It is yet another particular object of this invention to provide novel enamines.

It is a still further object of this invention to provide a novel process for producing polymers having acetylenic linkages.

It is still a further object of this invention to provide novel polymers incorporating acetylenic linkages.

In accordance with one aspect of the invention there is provided a process for producing a chemical intermediate for polymer manufacture comprising: reacting a Schiff's base of formula (III):

    Ar.sub.1 CH═NAr.sub.2                                  (III)

with an N-arylmethylheterocycle of formula (IV):

    Ar.sub.3 --CH.sub.2 --N                                    (IV)

in a basic medium wherein Ar₁, Ar₂ and Ar₃ are each independently selected from aryl and hetaryl, unsubstituted or substituted, one or more times, by radicals selected from F, Cl, Br; alkyl of 1 to 6 carbon atoms; alkenyl of 2 to 6 carbon atoms; aryl of 6 to 12 carbon atoms; aralkyl of 7 to 18 carbon atoms; aralkenyl of 8 to 18 carbon atoms, alkoxy of 1 to 6 carbon atoms; thioalkoxy of 1 to 6 carbon atoms; aryloxy of 6 to 12 carbon atoms; and thioaryloxy of 6 to 12 carbon atoms; and --N is a hetaryl radical.

If the process is operated under conditions favouring the elimination of the heterocyclic of formula (V):

    H--N                                                       (V)

the reaction proceeds to form a diarylacetylene of formula (I):

    Ar.sub.1 --C.tbd.C--Ar.sub.3                               (I)

in which Ar₁ and Ar₃ are as defined above, as the favoured reaction.

If the process is operated under conditions which do not favour elimination of the heterocyclic of formula (V):

    H--N                                                       (V)

the reaction forms an enamine of formula (II): ##STR4## wherein Ar₁, Ar₃ and --N are all as defined above.

In another aspect of the invention there is provided enamines of formula (II), as defined above.

In yet another aspect of the invention there is provided a process for producing diarylacetylenes from the enamines (II).

In still another aspect of the invention there is provided a process of producing polymers and copolymers incorporating acetylenic compounds.

In yet another aspect of the invention there is provided novel polymers and copolymers having acetylenic groups incorporated therein.

DESCRIPTION OF PREFERRED EMBODIMENTS

i) Synthesis of Intermediates

A novel synthesis of the invention comprises the reaction of the Schiff's base of formula (III), as defined above with the N-arylmethylheterocycle of formula (IV), as defined above in a basic medium.

This reaction can produce a diarylacetylene of formula (I), as defined above, or an enamine of formula (II), as defined above, or a mixture containing both.

The hetaryl radical --N is, in particular, one which behaves as a pseudohalogen, and if the reaction conditions favour elimination of the heterocycle of formula (V):

    H--N                                                       (V)

the reaction proceeds with formation of the diarylacetylene (I) as the major reaction product, whereas if the reaction conditions do not favour elimination of heterocycle (V), the reaction proceeds with formation of the enamine (II) as the major reaction product.

In general, higher reaction temperatures in conjunction with strongly basic conditions favour the elimination reaction which results in the diarylacetylene (I) as the major reaction product. In contrast, lower reaction temperatures in conjunction with weakly basic conditions do not favour the elimination reaction, thus leading to the enamine (II) as the major reaction product.

Reaction time is also a factor in determining whether the diarylacetylene (I) or the enamine (II) is the dominant reaction product.

Depending on the inter-relationship between these different process parameters, the reaction product may be predominantly the diarylacetylene (I) or the enamine (II), or a mixture of both in varying proportions.

The reaction resulting in the diarylacetylene (I) proceeds via the enamine (II) as an intermediate. The diarylacetylene (I) can be produced from the intermediate enamine (II) in situ, or the enamine (II) can be recovered or isolated from the reaction medium and subjected to conditions favouring formation of the diarylacetylene (I).

Thus the invention contemplates reaction of the Schiff's base (III) and the N-arylmethylheterocycle (IV) under basic conditions favouring elimination of the heterocycle (V) so that the reaction proceeds to the diarylacetylene (I) via the enamine (II). The invention also contemplates reaction of (III) and (IV) under first basic conditions which do not favour elimination of the heterocycle (V) to produce the enamine (II), and thereafter, possibly with prior isolation of the enamine (II), reacting the enamine (II) under second basic conditions effective for elimination of the heterocycle (V) to produce the diarylacetylene (I).

The invention also contemplates the elimination process in which the diarylacetylene (I) is produced from the enamine (II), as starting material.

ii) Process Parameters for Synthesis

The synthesis i) is carried out under basic conditions, more especially in a basic medium.

In particular, the medium suitably comprises a polar, aprotic organic solvent, for example, dimethylformamide, dimethylacetamide or N-methylpyrrolidone, which medium is rendered basic. The base character may be achieved by the presence of a base, for example, sodium or potassium tert-butoxide, sodium amide or sodium dimethyl amide; the sodium dimethyl amide may be generated in situ from sodium in N,N-dimethyl formamide. Mixtures of the bases may be employed.

As indicated above the base selected plays a role in determining whether the formation of the diarylacetylene (I) or the enamine (II) is favoured.

Since some heterocycles (V) have a strongly acidic character, the heterocycle (V) formed as a by-product of the formation of the diarylacetylene (I) from the enamine (II), may act as a buffer in the reaction medium, weakening the basic character and favouring termination of the reaction with formation of enamine (II).

The synthesis can be carried out conveniently at temperatures in the range of 0° to 100° C.; while still lower or higher temperatures outside this range can be employed; there is no advantage in employing temperatures outside this range.

In general lower temperatures in the range favour the first stage of the reaction to produce enamine (II) as the major reaction product. On the other hand, higher temperatures alone do not dictate continuation of the reaction through the enamine (II) to the diarylacetylene (I); and at the higher temperatures, the reaction time and the strength of the basic character of the reaction medium play a significanat role in determining which reaction product, (I) or (II), dominates; and, as indicated above, when considering the basic character of the reaction medium, it is not only the strength of the base employed which is to be considered, because the acidity of by-product heterocycle (V) also affects the basic character.

On the other hand, a surprisingly fast reaction to form a high yield of diarylacetylene (I) has been observed employing a basic reaction medium of potassium t-butoxide in dimethylformamide even when benzotriazole, which is strongly acidic, was formed as the by-product heterocycle (V). At a temperature of 75° C. the reaction proceeded to form the diarylacetylene in high yield in a reaction time of less than 1 minute.

At lower temperatures, however, the benzotriazole released buffered the reaction to favour the enamine (II) as the reaction product.

The rapid reaction with benzotriazole as the heterocyclic (V) presumably results from the high electron withdrawing character of the benzotriazolyl radical.

iii) Reactants

The Schiff's bases (III) are readily produced in condensation reactions between aromatic aldehydes and aromatic amines, a reaction fully described in prior literature.

The N-arylmethylheterocycles (IV) are readily produced by the reaction between arylmethylhalides and aromatic heterocyclic compounds under conditions for elimination of hydrogen halide, a reaction fully described in prior literature.

The aryl radicals Ar₁, Ar₂ and Ar₃ are suitably aromatic radicals having 6 to 16 carbon atoms in the aromatic nucleus, independently selected from: ##STR5## wherein x and y are integers independently selected from 0, 1, 2 or 3, z is an integer independently selected from 0, 1 or 2 and R, R' and R" are each independently selected from halogen atoms selected from fluorine, chlorine and bromine; alkyl of 1 to 6 carbon atoms, alkenyl of 2 to 6 carbon atoms; aryl of 6 to 12 carbon atoms, aralkyl of 7 to 18 carbon atoms; aralkenyl of 8 to 18 carbon atoms; alkoxy of 1 to 6 carbon atoms; thioalkoxy of 1 to 6 carbon atoms; aryloxy of 6 to 12 carbon atoms and thioaryloxy of 6 to 12 carbon atoms.

The hetaryl radicals Ar₁, Ar₂ and Ar₃ may be, for example, pyridinyl, furanyl, thiophenyl, thiazolyl or quinolinyl, which may be unsubstituted or substituted in the manner of the aryl radicals described above; for example the radicals: ##STR6##

The heterocyclic radical:

    --N

may be, for example, a benzimidazolyl, benzotriazolyl, triazolyl or tetrazolyl, which radicals may be unsubstituted or substituted. It will be understood that the nature of the substituent is immaterial, provided that it does not interfere with the reaction to produce the desired enamine (II) or diarylacetylene (I).

iv) Polymer Production Diarylacetylenes of formula (VI):

    X.sub.1 --Ar.sub.4 --C.tbd.C--Ar.sub.5 --X.sub.2           (VI)

in which X₁ and X₂ are independently selected from F and OH, and Ar₄ and Ar₅ are aryl or hetaryl as defined for Ar₁ and Ar₃, are starting materials for producing polymers which incorporate acetylenic groups.

The diarylacetylenes (VI) in which X₁ and X₂ are both fluorine are within formula (I) and are produced by the previously described synthesis of the invention.

The diarylacetylenes (VI) in which at least one of X₁ and X₂ is a hydroxyl are produced from the corresponding diarylacetylenes (VI) in which X₁ and X₂ are fluorine, by hydrolysis of one or both fluorine substituents or etherification of one or both fluorine substituents and hydrolysis of the resulting alkoxy or aryloxy substituents.

The reaction to replace one or both fluorine substituents by an alkoxy or aryloxy is a novel reaction and it was surprising that such reaction would proceed efficiently. It appears that the acetylenic linkage activates the fluorine atom, facilitating its displacement, but this was not to have been expected. The reaction proceeds efficiently in the presence of an alkali metal alkoxide or aryloxide in a polar, aprotic organic solvent. The reaction is illustrated in the following scheme ##STR7## in which X is H or F and R is alkyl or aryl, and Ar₄ and Ar₅ are as defined previously.

The production of homopolymers and copolymers, particularly poly(arylether)s, polyesters, polycarbonates and polyformals from diarylacetylenes (VI) is illustrated below: ##STR8##

In these reactions n is an integer indicating the length of the polymer chain.

Any bisphenol can be employed as the reactant HO--Ar--OH in the production of the poly(arylether). The radical Ar¹ is an aromatic moiety such as diphenylsulfone or benzophenone. When X is fluorine Ar₁ can also be a heterocyclic which activates the fluorine for nucleophilic substitution, for example, pyridine, benzoxazole, quinoxaline, an isoquinoline or a phthalazine.

Thus in another aspect of the invention there is provided a process for producing an acetylenic group-containing polymer or copolymer of the formula (VII): ##STR9## wherein Z₁ is fluorine, hydroxyl or mercaptyl, Z₂ is hydrogen or fluorine, Z₃ is --O--, --S--, --CH₂ --, --CO--, --CO--Ar₆ --CO-- or --Ar₇ --, in which Ar₆ and Ar₇ are selected from divalent aromatic linkages, Y₁ and Y₂ are each selected from --O-- and --S--, provided that when Z₃ is --O-- or --S--, Y₁ and Y₂ are both single bonds, Ar₄ and Ar₅ are each independently selected from arylene and hetarylene, unsubstituted or substituted one or more times by radicals selected from F, Cl, Br, alkyl of 1 to 6 carbon atoms; alkenyl of 2 to 6 carbon atoms; aryl of 6 to 12 carbon atoms; aralkyl of 7 to 18 carbon atoms; aralkenyl of 8 to 18 carbon atoms, alkoxy of 1 to 6 carbon atoms, thioalkoxy of 1 to 6 carbon atoms, aryloxy of 6 to 12 carbon atoms and thioaryloxy of 6 to 12 carbon atoms; X is --Ar₄ --C.tbd.C--Ar₅ or a copolymer unit, n is an integer of 2 to 200, x is an integer of 0 to 199 and n is >x.

It will be understood that the two basic units of (VII) may be in a random or non-random arrangement or sequence in the case of a copolymer.

In still another aspect of the invention there is provided an acetylenic group-containing polymer or copolymer of formula (VII) as defined above provided that when the polymer or copolymer has acetylenic units --Ar₄ --C═C--Ar₅ -- at both terminal positions, n is at least 3.

The divalent linkages --Ar₇ -- are in particular derived from dihydroxy aromatics, for example, bisphenols, or from dihaloaromatics in which the halo groups are activated by the presence of electron withdrawing groups such as sulphonyl or carbonyl groups.

Aromatic groups having electron withdrawing groups are thus, for example:

    --Ar--CO--Ar--

and

    --Ar--SO.sub.2 --Ar--

which the Ar groups are the same or different and are arylene or hetarylene.

The divalent aromatic linkages Ar₆ are selected from a broader class than Ar₇ since no electron withdrawing group is required in Ar₇.

The radical Ar of the bisphenols HO--Ar--OH may in particular be a radical of formula: ##STR10## in which R is hydrogen, lower alkyl of 1 to 6 carbon atoms or aryl of 6 to 10 carbon atoms, for example, phenyl or naphthyl; whereby homopolymers are produced of formula: ##STR11##

The divalent linkage Ar₇ may also be selected from the group Ar.

The copolymer unit X may be derived from a wide variety of comonomers, for example, the following comonomer units in which the free valancies are in ortho or para positions: ##STR12## in which Ar₁, Ar₂, Ar₃ and Ar₄ are independently selected from unsubstituted and substituted aryl. ##STR13## in which Ar₁, Ar₂, Ar₃ and R₄ are as defined above and Ar is aryl. ##STR14## in which R₂ is alkylene or arylene ##STR15##

The aromatic moieties of the dihydroxy aromatics may be, for example, arylene and biarylene moieties including the following: ##STR16##

Particular copolymers may be represented by the formula: ##STR17##

The halogen of the precursor dihaloaromatics may be fluorine, chlorine or bromine.

The diarylacetylenes (I) as a class can be readily oxidized to corresponding benzils useful in synthesis of a variety of polymers including polyquinoxalines, polyphenyls and phthalic anhydrides and the latter can be reacted with diamines to produce polyimides.

The enamines (II) of the invention are useful for the production of deoxybenzoins which can be oxidized to benzils which have utility in the production of polymers. The processes, involving use of enamines, described in U.S. Pat. No. 5,011,998, the teachings of which are hereby incorporated herein by reference, apply to the enamines (II) of the present invention.

Thus deoxybenzoins, benzils and polymers may be produced using the enamines (II) of this invention, and the procedures described in U.S. Pat. No. 5,011,998, incorporated herein by reference.

EXPERIMENTAL ##STR18## I. Synthesis of N-Benzyl-substituted Heterocyclics EXAMPLE 1 (Phenylmethyl)-1H-benzimidazole

To benzyl chloride (13 g, 0.103 mol), 1H-benzimidazole (11.81 g, 0.10 mol), K₂ CO₃ (60 g, 0.434 mol) was added acetonitrile (200 mL) and the mixture was stirred and heated under reflux for 3 h, filtered hot, and washed with hot CH₃ CN (100 mL). The solvent of the filtrate was evaporated and the residual mass recrystallized as needles (16.5 g, 79%): mp 119°-120° C. (benzene) (lit¹ mp 105° C.); ¹ H NMR (270 MHz, CDCl₃) δ5.40 (s, 2H, CH₂), 7.20-7.41 (m, 8H), 7.85-7.89 (m, 1H), 8.02 (s, 1H, NCHN); IR (CDCl₃) 3093 (w), 3065 (w), 3037 (w), 2929 (w), 1615 (w), 1496 (s), 1456, 1385 (w), 1361, 1331, 1285, 1261, 1204, 1181, 1007 (w), 963 (w), 947 (w) cm¹. MS (EI) m/e 208 (M⁺, 57.8), 91 (100); Anal. Calcd for C₁₄ H₂₂ N₂ (208.26): C, 80.74; H, 5.81; N, 13.45; Found: C, 80.70; H, 6.02; N, 13.31.

EXAMPLE 2 (Phenylmethyl)-1H-benzotriazole

(Phenylmethyl)-1H-benzotriazole was prepared from 1H-benzotriazole (11.91 g, 0.100 mol) and benzyl chloride as in Example 1 for 1 hour to give the title compound and (phenylmethyl)-2H- benzotriazole in a ratio of 75:25. Workup and two recrystallization gives the pure 1H-isomer: mp 117°-119° C. (CH₃ CN); (lit.¹ mp 114°-117° C.; lit.²,3 mp 115°-116° C.)

EXAMPLE 3 (Phenylmethyl)-1H-[1,2,4-triazole]

(Phenylmethyl)-1H-[1,2.4-triazole] was prepared from 1H-[1,2,4-triazole] (69.7 g, 0.100 mol) and benzyl chloride as in Example 1 for 1 hour to give the title compound and (phenylmethyl)-2H-[1,2,4-triazole]. Workup and recrystallization gave the pure 1H-isomer (54%): mp 52°-53° C. (cyclohexane); (lit.¹ mp 54° C.).

EXAMPLE 4 (2-Naphthalenyl)methyl-1H-benzotriazole

A procedure similar to Example 2 from 1H-benzotriazole and 2-naphthylmethyl chloride gave the title compound after recrystallization in 45% yield: mp 152°-153° C. (CH₃ CN); ¹ H NMR (200 MHz, CDCl₃) δ6.03 (s, 2H, CH₂), 7.32-7.38 (m, 4H), 7.48-7.53 (m, 2H), 7.77-7.83 (m 4H), 8.07-8.12 (m, 1H).

EXAMPLE 5 (1-Naphthalenyl)methyl-1H-benzotriazole

A procedure similar to Example 2 from 1H-benzotriazole and 1-naphthylmethyl chloride gave the title compound after recrystallization in 85% yield: mp 149°-151° C. (EtOAc/petroleum ether 35°-611° C. abbreviated elsewhere as PE); ¹ H NMR (200 MHz, CDCl₃) δ6.36 (s, 2H, CH₂), 7.29-7.59 (m, 7H), 7.87-7.93 (m, 2H), 8.06-8.11 (m, 1H), 8.21-8.26 (m 1H).

EXAMPLE 6 (4-Fluorophenyl)methyl-1H-benzotriazole

In a procedure as in Example 2 but using 1H-benzotriazole (23.8 g, 0.200 mol), 1-(chloromethyl)-4-fluorobenzene (29.0 g,0.200 mol) and K₂ CO₃ (70 g) in CH₃ CN (300 mL) for 1 hour gave the title compound and (4-fluorophenyl)methyl-2H-benzotriazole. Workup and recrystallization gave the mixture of the 1H and 2H-isomers (75% yield) which was used in the subsequent reactions. A sample (5 g) was chromatographed (PE/EtOAc 9:1) eluting first the 2H isomer and then the title compound: mp 92°-94° C. (cyclohexane); ¹ H NMR (300 MHz, CDCl₃) δ5.82 (s, 2H, CH₂), 7.00-7.06 (m, 2H), 7.25-7.46 (m, 5H), 8.08 (d, J=8.9 Hz, 1H); IR (CDCl₃) 3052 (w), 2938 (w), 1609, 1513, 1451 (w), 1351 (w), 1315 (w), 1269 (w), 1230 (s), 1159, 1084 cm⁻¹. MS (EI) m/e 227 (M⁺, 52.6), 198 (100), 109 (96.9); Anal. Calcd for C₁₃ H₁₀ N₃ F (227.24): C, 68.71; H, 4.44; F, 8.36; N, 18.49; Found: C, 68.44; H. 4.44; F, 8.40; N, 18.57.

EXAMPLE 7 (3-Fluorophenyl)methyl-1H-benzotriazole

In a procedure as in Example 2 but using 1H-benzothiazole (20.6 g, 0.173 mol), 1-(chloromethyl)-3-fluorobenzene (25.0 g, 0.173 mol), K₂ CO₃ (35.9 g) and CH₃ CN (1.50 mL) for 1h gave the title compound and (3-fluorophenyl)methyl-2H-benzotriazole. Similar workup and recrystallization gave the pure 1H-isomer (73%): mp 103°-104° C. (cyclohexane); ¹ H NMR (270 MHz, CDCl₃) δ5.87 (s, 2H, CH₂), 6.97-7.08 (m, 3H), 7.29-7.49 (m, 4H), 8.10 (d, J=8.0 Hz, 1H); Anal. Calcd for C₁₃ H₁₀ N₃ F (227.24): C, 68.71; H, 4.44; Found: C, 68.40; H, 4.67.

EXAMPLE 8 (2-Fluorophenyl)methyl-1H-benzotriazole

In a procedure as in Example 2 but using 1H-benzotriazole (34.5 g, 0.289 mol) and 1-(chloromethyl)-2-fluorobenzene (41.8 g, 0.289 mol) for 1h gave the title compound and (2-fluorophenyl)methyl-2H-benzotriazole in a ratio of 80:20. Similar workup and recrystallization gave the pure 1H-isomer (73%): mp 93°-95° C. (cyclohexane); ¹ H NMR (270 MHz, CDCl₃) δ5.93 (s, 2H, CH₂), 7.08-7.47 (m, 7H), 8.10 (d, J=7.2 Hz, 1H).

II. Synthesis of Schiff Bases ##STR19##

EXAMPLE 9 N-[(4-fluorophenyl)methylene]benzenamine

To 4-fluorobenzaldehyde (24.8 g, 0.200 mol) and aniline (18.6 g, 0.200 mol) was added benzene (200 mL) and acetic acid (0.7 mL) and the mixture is heated under reflux until all the water (3.6 mL) was azeotropically removed. The solvent is evaporated and the residual oil upon cooling and stirring crystallized. The white mass was then recrystallized as needles (28 g, 70%): mp 39°-40° C. (PE) (lit.¹ mp 40° C.).

EXAMPLE 10 N-[(3-fluorophenyl)methylene]benzenamine¹,2

A similar procedure as for the preparation of N-[(4-fluorophenyl)methylene]benzenamine (no acetic acid required) gave an oil which was distilled (87%): bp 100°-101° C./0.75 mm Hg.

EXAMPLE 11 N-[(2-fluorophenyl)methylene]benzenamine

A similar procedure as for the preparation of N-[(4-fluorophenyl)methylene]benzenamine (no acetic acid required) gave an oil which was distilled (90%): bp 103°-104° C./1.5 mm Hg pressure; (lit.¹ bp 135° C.).

III. Synthesis of Enamines ##STR20##

(1,2-diphenylethenyl)-1H-benzotriazole EXAMPLE 12 Method 1

To a mixture of powdered KOH (2.24 g, 0.040 mol) and DMF (18 mL) there was added with rapid stirring phenylmethyl-1H-benzotriazole (1.05 g, 0.005 mol) and N-phenylmethylenebenzenamine (0.905 g, 0.005 mol) in DMF (7 mL) at 75° C. After five minutes the reaction was poured into ice-cold water (75 mL) and left to crystallize the title enamine. This was filtered, washed with water, and dried to yield 1.07 g (72%) of the title enamine. An analytical sample was chromatographed PE/EtOAc 4:1 and recrystallized with charcoal treatment: mp 152°-154° C. (cyclohexane); Anal. Calcd for C₂₀ H₁₅ N₃ (297.36): C, 80.78; H, 5.08; N, 14.13; Found: C, 80.66; H, 5.14; N, 14.14.

EXAMPLE 13 Method 2

A procedure similar to Example 12 except that instead of KOH potassium t-butoxide (0.56 g, 0.005 mol) was used. At 75° C. the reaction was complete and worked up as above. Chromatography first with PE elutes some (5-10%) diphenyl acetylene and then PE/EtOAc 4:1 elutes the title enamine (75-80%). This method was applied to other bases as given in Table 1.

EXAMPLE 14 (1,2-Diphenylethenyl)-1H-benzimidazole

A procedure as in Example 13 using (phenylmethyl)-1H-benzimidazole gave the enamine (82%): mp 141°-143° C. (cyclohexane); ¹ H NMR (300 MHz, CDCl₃) δ6.82 (m, 2H), 6.98 (d, J=8.0 Hz, 1H), 7.14-7.19 (m, 5H), 7.25-7.38 (m, 6H), 7.83 (s, 1H, NCHN), 7 (88, J=d, 9.0 Hz, 1H); IR (CDCl₃) 3085 (w), 3063, 3032 (w), 1635, 1611 (w), 1491 (s), 1484, 1452, 1391, 1365 (w), 1308, 1284, 1259, 1218, 1183 (w), 1078 (w), 1031 (w), 1006 (w) cm¹. MS (EI) m/e 296 (M⁺, 100), 219 (13), 178 (52); Anal. Calcd for C₂₁ H₁₆ N₂ (296.38): C, 85.11; H, 5.44; N, 9.45; Found: C, 85.03; H, 5.50; N, 9.45.

EXAMPLE 15 [1,2-bis(4-fluorophenyl)ethenyl)]-1H-benzotriazole

A procedure as in Example 13 using (4-Fluorophenyl)methyl-1H-benzotriazole. gave the title enamine (60%): mp 134°-136° C. (cyclohexane); MS (EI) m/e 333 (M+, 5), 305 (50), 304 (100), 303 (32), 215 (20), 214 (23), 183 (62); Anal. Calcd for C₂₀ H₁₃ F₂ N₃ (333.34): C, 72.06; H, 3.93; F, 11.4; N, 12.61; Found: C, 72.28; H, 3.93; F, 11.11; N, 12.74.

IV. Synthesis of Acetylenes ##STR21##

Diphenylacetylene. General Procedure EXAMPLE 16 Method a

To potassium t-butoxide (3.36 g, 30 mmol) in DMF (40 mL) at 75° C. was added as quickly as possible and all at once the [arylmethyl]-1H-benzotriazole (10 mmol) and N-(arylmethylene)benzenamine (10 mmol) dissolved in DMF (10 mL). Within a minute the solution is poured into ice-cold water (150 mL), extracted with CHCl₃ (3×50 mL) and chromatographed (PE). The acetylenes were recrystallized from MeOH. Thus was obtained: diphenylacetylene (75 %): mp 59°-61° C. (MeOH); IR (CDCl₃) 1650 (w), 1604 (w), 1589 (w), 1512 (s), 1233, 1155 (w) cm⁻¹.

EXAMPLE 17 Method b

To potassium t-butoxide (5.6 g, 50 mmol) in DMF (40 mL) at 75° C. was added N-(phenylmethyl)-1H-benzimidazole (2.08 g, 10 mmol) and N-(phenylmethylene)benzenamine (1.81 g, 10 mmol) dissolved in DMF (10 mL). After 5 hours the solution is poured into ice-cold water (150 mL), extracted with CHCl₃ (3×50 mL) and chromatographed (PE). Diphenylacetylene was obtained in 73 % yield.

EXAMPLE 18 Method c

To potassium t-butoxide (5.6 g, 50 mmol) in DMF (40 mL) at 75° C. was added N-(phenylmethyl)-1H-1,2,4-triazole (1.59 g, 10 mmol) and N-(phenylmethylene)benzenamine (1.81 g, 10 mmol) dissolved in DMF (10 mL). After 30 minutes the solution is poured into ice-cold water (150 mL), extracted with CHCl₃ (3×50 mL) and chromatographed (PE). Diphenylacetylene was obtained in 11% yield.

                                      TABLE 1                                      __________________________________________________________________________     Influence of different bases and temperatures on the reaction of phenyl-       methy-1H-benzotriazole (5 mmol) and N-phenylmethylenebenzenamine (5            mmol)                                                                          in DMF (25 mL) in the production of the enamine (1) and diphenylacetylene      (2).                                                                                 Temp.                                                                               Time Base (mmol)           Yield (%)                                Example                                                                              (°C.)                                                                        (min)                                                                               NaNH2 Na  t-BuOH                                                                               KOt-Bu                                                                               1  2                                     __________________________________________________________________________     19    75   30   0     22  0     0      0 55                                    20    75   50   0     4.8 2.3   0     55 5                                     21    60   30   0     9.1 4.6   0     61 0                                     22    75   60   0     4.8 0     0     32 0                                     23    50   20   0     0   0     5     40 35                                    24    22   20   0     0   0     2.5   60 0                                     25     0   80   0     0   0     3.57  56 0                                     26    75   70   15    0   0     0     47 5                                     27    75   1100 0     22  11    0      3 42                                    __________________________________________________________________________

EXAMPLE 28 1-(Phenylethynyl)naphthalene

In a procedure similar to that of Example 16 using [phenylmethyl]-1H-benzotriazole (10 mmol) and N-([1-naphthalenyl]methylene)benzenamine (10 mmol): 88% yield: mp 51°-53° C. (MeOH) (lit¹ oil); ¹ H NMR (300 MHz, CDCl₃) δ7.39-7.69 (m, 8H), 7.77-7.90 (m, 3H), 8.46 (br d, 2.7H, 1H); IR (CDCl₃) 3060 (s), 2245 (eyne), 1596, 1581, 1508, 1491 (s), 1442, 1398, 1333, 1215, 1070, 1017 cm¹. MS (EI) m/e 228 (M⁺, 100).

EXAMPLE 29 1-Methoxy-4-(phenylethynyl)benzene

Procedure similar to that of Example 16 using [phenylmethyl]-1H-benzotriazole (10 mmol) and N-[(4-methoxyphenyl)methylene]benzenamine (10 mmol): 67% yield: mp 57°-58° C. (MeOH) (lit.¹ 58°-60° C.); ¹ H NMR (300 MHz, CDCl₃) δ3.84 (s, 3H, OCH₃), 6.89 (d, 1.9H, 2H, C(3 and 5)H), 7.30-7.38 (m, 3H), 7.45-7.54 (m, 4H).

EXAMPLE 30 Bis(4-fluorophenyl)acetylene

To potassium t-butoxide (1.5 g, 13.4 mmol) in DMF (15 mL) at 75° C. was added as quickly as possible and all at once [(4-fluorophenyl)methyl]-1H-benzotriazole (1.14 g, 5 mmol) and (4-fluorophenyl)methylenebenzenamine (1.00 g, 5 mmol) dissolved in DMF (10 mL). Within a minute the solution is poured into ice-cold water (75 mL) crystallizing the title compound which was filtered and then chromatographed (PE). The acetylene 0.54 g (50%) recrystallizes as needles: mp 95°-96° C. (MeOH); (lit.¹ 94°-95° C.).

EXAMPLE 31 4-(t-Butoxy)-4'-fluorodiphenylacetylene

A similar procedure as for the preparation of bis(4-fluorophenyl)acetylene in Example 30 but stirred at 75° C. for 15 min and then quenched with water gave the title acetylene (15% HPLC) and bis(4-fluorophenyl)acetylene (30% HPLC). Chromatography (PE) elutes the difluoro derivative then PE/EtOAc 97:3 elutes the title compound recrystallizing as colorless plates 2.5 g (10%): mp 102°-104° C. (MeOH); ¹ H NMR (200 MHz, CDCl₃) δ1.35 (s, 9H, (CH₃)₃), 6.93-7.06 (dd, J=8.6 Hz, 4H), 7.39-7.51 (m, 4H); IR (CDCl₃) 3020 (w), 2981, 2247 (w,(acetylenic stretch), 1605, 1515 (s), 1474 (w), 1393 (w), 1367, 1281 (w), 1234, 1218, 1157 (s) cm⁻¹. MS (EI) m/e 268 (M+ (4.5)), 212 (100), 183 (28), 157 (9.4); Anal. Calcd for C₁₈ H₁₇ FO (268.33): C, 80.57; H, 6.39; Found: C, 80.10; H, 6.42.

EXAMPLE 32 4,4'Bis(t-Butoxy)diphenylacetylene

A similar procedure as for the preparation of bis(4-fluorophenyl)acetylene.]in Example 30 but using 5 equiv of potassium t-butoxide for 150 minutes and then quenched with water gave the title acetylene (45% HPLC). Chromatography (PE/EtOAc 9:1) and recrystallization with charcoal treatment gave 0.64 g (40%) colorless prisms: mp 129°-131° C. (MeOH); ¹ H NMR (300 MHz, CDCl₃) δ1.36 (s, 18H, C(CH₃)₃), 6.96 (d, J=8.7 Hz, 4H, phenyl C3 and 3'H), 7.43 (d, 4H, phenyl C2 and 2'H); IR (CDCl₃) 3040 (w), 2980, 2936 (w), 2907, 2875, 1606, 1511, 1475 (w), 1394, 1367, 1309 (w), 1240, 1158 (s), 1101 (w), 1016 (w) cm⁻¹. MS (EI) m/e 322 (M⁺, 6.1), 266 (4.1), 210 (100).

EXAMPLE 33 1,2-Bis(4-hydroxyphenyl)-ethanone

To a solution of acetic acid (15 mL), c. HCl (2.0 mL) and H₂ O (3.0 mL) was added 1,1'-(1,2-ethynediyl)bis[4-(1,1-dimethylethoxy)benzene] (1.0 g, 3.1 mmol) and heated under reflux 1.5 h. Then the solution was poured into ice-cold H₂ O (50 mL) precipitating the title compound which was filtered washed with water, air-dried, and recrystallized into tanned needles (0.52 g, 80% yield). A second recrystallization with charcoal treatment and acidification of the solution gave colorless needles: mp 217°-220° C. (H₂ O) (lit¹ mp 214°-215° C.); ¹ H NMR (300 MHz, DMSO-d₆) δ4.09 (s, 2H, CH₂), 6.66 (d, J=8.45 Hz, 2H, C9H), 6.82 (d, J=8.7 Hz, 2H, C2H), 7.02 (d, 2H, C8H), 7.89 (d, 2H, C 3H), 9.23 (s, 1H, C10OH), 10.34 (s, 1H, C1OH); ¹³ C NMR (300 MHz, DMSO-d₆) δ43.44 (CH₂), 115.11, 115.20, 125.58, 127.85, 130.36, 130.54, 131.02, 131.17, 155.85, 161.97, 196.18 (C═O); MS (EI) m/e 228 (M⁺, 4), 121 (100), 107 (14.8), 93 (13), 65 (15).

EXAMPLE 34 1-Hydroxy-4-(phenylethynyl)benzene

A procedure similar to that described¹ was used. A sample of 1-methoxy-4-(phenylethynyl)-benzene (0.4 g, 1.9 mmol) was added collidine (3 mL), LiI (1.5 g) and the solution heated under reflux for 5 h (>95% conversion). The solution was poured into water acidified with HCl, extracted with ether (3×50 mL) and dried (MgSO₄). The ether was evaporated and the residue chromatographed (PE) eluting the title compound 0.3 g (80%): mp 125°-128° C. (cyclohexane) (lit² mp 91°-92° C., lit³ mp 83°-84° C.); ¹ H NMR (300 MHz, DMSO-d₆) δ6.80 (d, J=8.77 Hz, 2H, C2H), 7.37 (d, 2H, C3H), 7.35-7.42 (m, 3H), 7.46-7.50 (m, 2H), 9.92 (s, 1H, OH); ¹³ C NMR (300 MHz, DMSO-d₆ ) δ87.32 (acetylenic C), 89.98 (acetylenic C), 112.42 (sp² C), 115.74, 122.90 (sp² C), 128.20, 128.66, 131.06, 133.00, 158.06 (COH); IR (CDCl₃) 3596 (OH), 3066 (w), 3039 (w), 2217 (w, acetylenic stretch), 1605, 1512, 1429 (w), 1328 (w), 1261 (s), 1219, 1171 (s), 1140 (w), 1099 (w), 834, 805 (w) cm⁻¹. MS (El) m/e 194 (M⁺, 100), 165 (29.4), 97 (11.3).

EXAMPLE 35 4,4'-Bis(phenoxy)diphenylacetylene

To 4,4'-difluorotolane (0.5 g, 0.0023 mol) and dry potassium phenolate (prepared from aqueous KOH and phenol with azeotropic removal of H₂ O with benzene) (1.5 g, 0.011 mol) was added DMF (10 mL) and the mixture heated at 170° C. for 12 h after which there appeared a little difluorotolane remaining. This mixture was poured in water, the precipitate was filtered, washed with water, dried, and the title compound recrystallized as flakes 0.54 g (64%): mp 171°-173° C. (acetic acid) (lit.¹ mp 167°-168° C.); ¹ H NMR (270 MHz, CDCl₃) δ6.89 (d, J=8.7 Hz, 4H, phenylene C3,3'H), 6.97 (d, J=8.6 Hz, 4H, phenyl C2,2'H), 7.07 (t, J=7.9 Hz, 2H, phenyl C4H), 7.29 (t, 4H, phenyl C3,3'H), 7.40 (d, 4H, phenylene C2,2'H); IR (CDCl₃) 3041 (w), 3020 (w), 1590, 1512, 1488, 1312 (w), 1274 (w), 1238 (s), 1218, 1165 (w), 1020 (w) cm⁻¹. When the sample is placed in a DSC apparatus with a N₂ gas flow ramped at 10° C./min it shows a Tm=163.9° C. In a gas-tight crucible and the temperature ramped at 2° C./min this sample shows Tm=169.5° C. and an exotherm maximum at 359.3° C. The exotherm begins at ˜302° C. and ends at ˜396° C. Some of this material is heated in a closed glass capillary tube at 320°-330° C. for 6 h and then an aliquot of the product was chromatographed (HPLC). The retention times (tR in rain) and area % were: 4.43 (8), 4.63 (6), 9.02 (40), 13.08 (6.5), 19.24 (1.5).

EXAMPLE 36 3,3'-Difluorodiphenylacetylene

A similar procedure to Example 30 but using [(3-fluorophenyl)methyl]-1H-benzotriazole and (3-fluorophenyl)methylenebenzenamine, gave the title acetylene after recrystallization (30%) needles: mp 60°-62° C. (MeOH) (lit.¹ mp 61°-62° C., lit.² mp 55.5-58° C.); ¹ H NMR (300 MHz, CDCl₃) δ7.04-7.11 (m, 2H), 7.22-7.25 (m, 2H), 7.31-7.35 (m, 4H); ¹³ C NMR (300 MHz, CDCl₃) δ88.89 (2.9, ethynyl C), 115.92 (21.1, C4), 118.42 (22.9, C2), 124.60 (9.5, C1), 127.54 (2.9, C6), 129.97 (8.7, C5), 162.36 (246.7, C3).

EXAMPLE 37 2,2'-Difluorodiphenylacetylene

A similar procedure to Example 30 but using [(2-fluorophenyl)methyl]-1H-benzotriazole and (2-fluorophenyl)methylenebenzenamine, gave the title acetylene after chromatography (PE) and recrystallization (1.5%) needles: mp 53°-54° C. (MeOH); ¹ H NMR (200 MHz, CDCl₃) δ7.05-7.16 (m, 4H), 7.27-7.38 (m, 2H), 7.50-7.58 (m, 2H); ¹³ C NMR (200 MHz, CDCl₃) δ88.05 (2.6, acetylenic C), 112.03 (15.8, C1), 116.02 (21, C3), 124.49 (3.8, C6), 130.83 (8, C4), 134.06 (C5), 163.24 (253, C2); IR (CDCl₃) 3040 (w), 2228 (w, acetylenic stretch), 1951 (w), 1917 (w), 1883 (w), 1799 (w), 1700 (w), 1615 (w), 1576, 1501, 1447 (s), 1413 (w), 1321 (w), 1264 (s), 1224 (S), 1155 (w), 1100, 1030 cm⁻¹. MS (El) m/e 214 (M⁺, 100), 107 (12.8).

EXAMPLE 38 2,4'-Difluorodiphenylacetylene

A similar procedure to Example 30 but using [(4-fluorophenyl)methyl]-1H-benzothiazole (1.14 g, 5 mmol) and (2-fluorophenyl)methylenebenzenamine (1.00 g, 5 mmol), gave the title acetylene after recrystallization (50%) needles: mp 108°-109° C. (MeOH); ¹ H NMR (200 MHz, CDCl₃) δ7.0-7.18 (m, 4H), 7.24-7.38 (m, 1H), 7.45-7.59 (m, 3H); ¹³ C NMR (200 MHz, CDCl₃) δ82.77 (acetylenic C1), 93.72 (3.35, acetylenic C1'), 112.21 (15.39, C1), 116.03 (21.07, C3), 116.16 (22.18, C3'), 119.50 (3.41, C1'), 124.50 (3.67, C6), 130.57 (8.04, C4), 133.99 (8.15, C5 or C2'), 134.16 (8.5, C 5 or C2'), 163.24 (252.45, C2 or C4'), 163.32 (250.7, C2 or C4'); IR (CDCl₃) 2263 (w), 2247 (ethynyl stretch, w), 1600 (C═C), 1574 (w), 1510 (s), 1489, 1451, 1264, 1228, 1156, 1096, 1029 (w) cm⁻¹. MS (EI) m/e 214 (M⁺, 100).

EXAMPLE 39 3,4'difluorodiphenylacetylene

A similar procedure to Example 30 but using [(4-fluorophenyl)methyl]-1H-benzotriazole (1.14 g, 5 mmol) and (3-fluorophenyl)methylenebenzenamine (1.00 g, 5 mmol), gave the title acetylene after recrystallization (60%) needles: mp 88°-89° C. (MeOH).

EXAMPLE 40 Bis(2-naphthyl)acetylene

A procedure similar to Example 16 using N-([2-naphthalenyl]methylene)benzenamine and 2-naphthylmethyl chloride gave a 76% yield of product: mp 225°-226° C. (MeOH) (lit.¹ mp 228°-229° C.).

EXAMPLE 41 Bis(1-naphthyl)acetylene

A procedure similar to Example 16 using N-([1-naphthalenyl]methylene)benzenamine and 1-naphthylmethyl chloride gavea 67% yield of product: mp 127°-128° C. (MeOH) (lit.¹ mp 129° C.).

EXAMPLE 42 Methylenebis(4-oxyphenylethynyl)bisbenzene

A procedure similar to Example 16 but using [phenylmethyl]-1H-benzotriazole (2.09 g, 10 mmol) and 4,4-methylenedioxybis(phenylmethylene)dianiline¹ (2.02 g, 5 mmol) for 1 h at 75° C. gave after chromatography (PE/EtOAc 4:1) the title acetylene (30%): mp 140°- 143° C. (cyclohexane); ¹ H NMR (200 MHz, CDCl₃) δ5.74 (s, 2H, CH₂), 7.05-7.10 (m, 4H), 7.30-7.35 (m, 6H), 7.45-7.52 (m, 8H); ¹³ C NMR (300 MHz, CDCl₃) δ88.58 (acetylenic C), 88.97 (acetylenic C), 90.70, 116.36, 117.41, 123.36, 128.08, 128.31, 131.48, 133.09, 156.72; IR (CDCl₃) 3062 (w), 2978 (w), 2911 (w), 2217 (w, acetylenic stretch), 1599, 1573 (w), 1509, 1443 (w), 1414 (w), 1314 (w), 1279 (w), 1233, 1209 (s), 1175, 1137 (w), 1103 (w), 1014, 836 cm⁻¹. MS (EI) m/e 400 (M⁺, 64), 207 (100), 194 (18.7), 177 (83.7), 165 (24.3), 151 (27.0).

EXAMPLE 43 2-(2-Phenylethynyl)furan

A procedure similar to Example 16 but with 2-(N-phenylaminomethylidine)-furan (0.86 g, 0.005 mol) and (phenylmethy)-1H-benzotriazole (1.05 g, 0.005 mol) gave after workup and chromatography (PE/EtOAc 4:1 ) an oil (90%, 98.5% pure) (lit.¹ oil bp 74° C./0.1 mm Hg) which darkened on standing: ¹ H NMR (270 MHz, CDCl₃) δ6.61 (dd, J=₃₄ 3.3,₂₃ 1.98 Hz, 1H, C3H), 6.855 (d, 1H, C4H), 7.52-7.55 (m, 3H, phenyl), 7.616 (d, 1H, C2H), 7.71 (m, 2H, phenyl); ¹³ C NMR (270 MHz, CDCl₃) δ79.38 (CC(C₄ H₄ O)), 93.22 (PhCC), 111.03 (C4), 115.19 (C3), 122.25 (C1'), 128.35 (C3'), 128.65 (C4'), 131.38 (C2'), 137.12 (C2), 143.59 (C5); MS (El) m/e 168 (M⁺, 100), 139 (96.8).

EXAMPLE 44 3-(2-Phenylethynyl)pyridine

A procedure similar to Example 16 but with 3-(N-phenylaminomethylidine)-pyridine (0.911 g, 0.005 mol) and (phenylmethy)-1H-benzotriazole (1.05 g, 0.005 mol) gave after workup and chromatography (PE/EtOAc 4:1) and treatment with boiling PE white needles (80%): mp 47°-48° C. (PE) (lit.¹ mp 47°-48.5° C., acetylenic stretch 2200 cm⁻¹); MS (EI) m/e 179 (M⁺, 100), 126 (21.7).

V. Synthesis of Indoles ##STR22##

EXAMPLE 45 1-Phenyl-2-(4-fluorophenyl)-1H-indole

A solution of (2-fluorophenyl)methyl-1H-benzotriazole (1.13 g, 5 mmol) and N-[(4-fluorophenyl)methylidine]benzenamine (0.996 g, 5 mmol) in DMF (7 mL) was stirred into potassium t-butoxide (1.68 g, 15 mmol) in DMF (18 mL) preheated to 75° C. The reaction monitore by HPLC showed completion upon mixing. After 11 minutes the DMF solution was poured in ice-cold H₂ O (75 mL) extracted with CHCl₃ (3×50 mL) and the solvent was evaporated. Chromatography first using PE as eluted 1-(4-fluorophenylethynyl)[2-fluorobenzene] (vide infra) then the eluant was changed to PE/EtOAc 97:3 eluting the title indole (40%): mp 126°-128° C. (MeOH); ¹ H NMR (200 MHz, CDCl₃) δ6.77 (s, 1H, C3H), 6.94 (t, J=8.7 Hz, 2H, phenic H), 7.16-7.48 (m, 10H), 7.66-7.72 (m, 1 H); MS (EI) m/e 287 (M⁺, 100).

VI. Polymer Synthesis ##STR23##

EXAMPLE 46 Poly(phenylene ether yne) from BPA

A mixture of 4,4'-(1-Methylethylidene)bisphenol (BPA) (1.141 g, 5 mmol), 4,4'-difluorodiphenylacetylene (1.071 g, 5 mmol) and anhydrous K₂ CO₃ (0.9 g, mmol) in toluene (10 mL) and N-methylpyrrolidinone (NMP) (14 mL) was stirred and heated to the reflux temperature of toluene azeotropically removing the water for 5 hours under a slow stream of N₂. The temperature was allowed to increase to 180° C. over a period of 5 hours allowing for the removal of toluene and NMP (4 mL). The dark mixture was then allowed to stir for an additional 10 hours when an aliquot flooded in MeOH precipitated high molecular weight polymer. The organics were cooled, filtered through celite, precipitated (MeOH),and dissolved in CHCl₃, filtered and reprecipitated (MeOH), washed (H₂ O) and dried to yield 1.57 g of the title polymer: Tg=163° C. exotherm maximum 398° C. (temperature ramped at 20° C./min), ηinh 0.69 dL/g (TCE, 25.4° C.), Mw=54400 Mn=23300. After a second scan there was no discernable glass transition temperature indicating that the polymer is now highly crosslinked. After heating the polymer is also now completely insoluble in all solvents.

Poly(phenylene ether yne)s were synthesized as in Example 46 using bisphenols and 2,4'-difluorodiphenylacetylene from Example 38 instead of 4,4'-difluorodiphenylacetylene.

    ______________________________________                                          ##STR24##                                                                                                   TGA                                              Bisphenol                     (T °C.-10% wt. loss)                      (HOArOH)      ηinh                                                                               Tg °C.                                                                          air     N.sub.2                                  ______________________________________                                         Example 47                                                                             BPA       0.39    142   456     411                                    Example 48                                                                             4,4'-biphenol                                                                            0.29    159   558     546                                    ______________________________________                                    

EXAMPLE 49 Poly(phenylene ether yne) from 4,4'-difluorodiphenylacetylene and bis(4-hydroxyphenyl)-9,9-fluorene ##STR25##

4,4'-Difluorodiphenylacetylene (2.1422 g, 0.01000 mol), bis(4-hydroxyphenyl)-9,9-fluorene (3.50416 g, 0.01000 mol), potassium carbonate (1.52 g, 0.0110 mol) NMP (28 mL) and toluene (20 mL) were heated at 140° C. for 1 h with removal of water with a Dean-Stark trap under a slow stream of nitrogen. The temperature was raised to 195° C. by bleeding toluene from the system and maintaining this temperature for 4.5 h. Heating was discontinued, NMP (15 mL) was added to the hot polymer mixture. This mixture was then added dropwise to a fast-stirring MeOH/H2O (600 mL:200 mL) mixture. The resulting precipitated polymer beads were suction-filtered, washed with water and MeOH and air-dried for 1 h. The material was dissolved in CHCl₃ (200 mL) and filtered through a bed of MgSO₄ (0.5 cm) and celite (4 cm) in a 150 mL fritted funnel and washed with CHCl₃ (200 mL). The volume of the filtrate was reduced to 100 mL and the title polymer was recovered by dropwise addition of this chloroform solution into MeOH (500 mL). The beads were filtered and air-dried over three days to give a quantitative yield of the title polymer, Tg=263° C. exotherm maximum 388° C. (temperature ramped at 20° C./min). After a second scan there was no discernable glass transition temperature indicating that the polymer is now highly crosslinked. After heating the polymer is also now completely insoluble in all solvents.

VII. Copolymer Synthesis ##STR26##

The following copolymers were synthesized as in Example 43 using the molar amounts of 4,4'-difluorodiphenylacetylene and 4,4'-dichlorodiphenylsulfone shown in Table 2.

                                      TABLE 2                                      __________________________________________________________________________     Properties of Copolymers                                                       n        m  Inherent                                                                             Tg  Tg after curing                                                                         TGA °C.                                  Example                                                                              mol % Viscosity                                                                            °C.                                                                         1 hr @ 340° C.                                                                   N2 (-10%) Air                                                                            Film Solubility                       __________________________________________________________________________     50     5 95 0.39  208 218      511  522  brittle                                                                             CH2Cl2/CHCl3                     51    10 90 0.4   210 225      526  530  brittle                                                                             CH2Cl2/CHCl3                     52    30 70 0.64  188 277      522  531  brittle                                                                             NMP/TCE (hot)                    __________________________________________________________________________ 

We claim:
 1. A process for producing an acetylenic group-containing polymer or copolymer of formula (VII): ##STR27## wherein Z₁ is fluorine, hydroxyl or mercaptyl, Z₂ is hydrogen or fluorine Z₃ is --O--, --S--, --CH₂ --, --CO--, --CO--Ar₆ --CO-- or --Ar₇ --, in which Ar₆ and Ar₇ are selected from divalent aromatic linkages, Y₁ and Y₂ are each selected from --O-- or --S--, provided that when Z₃ is --O-- or --S--, Y₁ and Y₂ are both single bonds, Ar₄ and Ar₅ are each independently selected from arylene or hetarylene, unsubstituted or substituted one or more times by radicals selected from F; Cl,; Br; alkyl of 1 to 6 carbon atoms; alkenyl of 2 to 6 carbon atoms; aryl of 6 to 12 carbon atoms; aralkyl of 7 to 18 carbon atoms; aralkenyl of 8 to 18 carbon atoms; alkoxy of 1 to 6 carbon atoms; thioalkoxy of 1 to 6 carbon atoms; aryloxy of 6 to 12 carbon atoms or thioaryloxy of 6 to 12 carbon atoms; X is --Ar₄ --C.tbd.C--Ar₅ or a copolymer unit, n is an integer of 2 to 200, x is an integer of 0 to 199 and n is >x, comprising:polymerizing a diarylacetylene of formula (VI):

    X.sub.1 --Ar.sub.4 --C.tbd.C--Ar.sub.5 --X.sub.2           (VI)

in which X₁ and X₂ are independently selected from F or OH and Ar₄ and Ar₅ are as defined above, or copolymerizing said diarylacetylene of formula (VI) with a comonomer selected from dihydroxy aromatics or dihaloaromatics in which the halogen atoms are activated for displacement, or in the presence of a reactant which provides a divalent linkage for the acetylenic monomer units, selected from --CH₂ --, --O--, --S--, --CO-- or said copolymer unit X.
 2. A process according to claim 1 in whichx is an integer 0; Ar₄ and Ar₅ are each independently selected from said unsubstituted or substituted arylene; Y₁ and Y₂ are both --O--; and Z₃ is said radical --Ar₇ -- in which --Ar₇ -- is a radical of formula: ##STR28## in which R is hydrogen, lower alkyl of 1 to 6 carbon atoms or aryl of 6 to 10 carbon atoms, which comprises polymerizing said diarylacetylene of formula (VI).
 3. A process according to claim 1 in whichx is an integer greater than 0; Ar₄ and Ar₅ are each independently selected from said unsubstituted or substituted arylene; Y₁ and Y₂ are both --O--; Z is said radical --Ar₇ -- in which --Ar₇ -- is a radical of formula: ##STR29## in which R is hydrogen, lower alkyl of 1 to 6 carbon atoms or aryl of 6 to 10 carbon atoms, and X is a radical of formula: ##STR30## which comprises copolymerizing said diarylacetylene of formula (VI) with a comonomer of formula: ##STR31## in which Y¹ and Y² are independently selected from hydroxy fluorine, chlorine or bromine.
 4. An acetylenic group-containing polymer or copolymer of formula (VII): ##STR32## wherein Z₁ is fluorine, hydroxyl or mercaptyl, Z₂ is hydrogen or fluorine, Z₃ is --O--, --S--, --CH₂ --, --CO--, --CO--Ar₆ --CO-- or --Ar₇ --, in which Ar₆ and Ar₇ are selected from divalent aromatic linkages, Y₁ and Y₂ are each selected from --O-- or --S--, provided that when Z₃ is --O-- or --S--, Y₁ and Y₂ are both single bonds, Ar₄ and Ar₅ are each independently selected from arylene or hetarylene, unsubstituted or substituted one or more times by radicals selected from F; Cl,; Br; alkyl of 1 to 6 carbon atoms; alkenyl of 2 to 6 carbon atoms; aryl of 6 to 12 carbon atoms; aralkyl of 7 to 18 carbon atoms; aralkenyl of 8 to 18 carbon atoms; alkoxy of 1 to 6 carbon atoms; thioalkoxy of 1 to 6 carbon atoms; aryloxy of 6 to 12 carbon atoms or thioaryloxy of 6 to 12 carbon atoms; X is Ar₄ --C.tbd.C--Ar₅ or a copolymer unit, n is an integer of 2 to 200, x is an integer of 0 to 199 and n is >x, provided that when the polymer or copolymer has acetylenic units --Ar₄ --C.tbd.C--Ar₅ at both terminal positions, n is at least
 3. 5. An acetylenic group-containing polymer according to claim 4 in whichx is an integer 0; Ar₄ and Ar₅ are each independently selected from said unsubstituted or substituted arylene; Y₁ and Y₂ are both --O--; and Z₃ is said radical --Ar₇ -- in which --Ar₇ -- is a radical of formula: ##STR33## in which R is hydrogen, lower alkyl of 1 to 6 carbon atoms or aryl of 6 to 10 carbon atoms.
 6. An acetylenic group-containing copolymer according to claim 4 in whichx is an integer greater than 0; Ar₄ and Ar₅ are each independently selected from said unsubstituted or substituted arylene; Y₁ and Y₂ are both --O--; Z is said radical --Ar₇ -- in which --Ar₇ -- is a radical of formula: ##STR34## in which R is hydrogen, lower alkyl of 1 to 6 carbon atoms or aryl of 6 to 10 carbon atoms, and X is a radical of formula: ##STR35## 